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Superta E

EUDAMED

Class I (EU MDR)

Ref SUPERTA-E-90

by PROMA REHA, s.r.o.

Identity

Trade Name
SUPERTA E EUDAMED
Device Name
Kinetic bed EUDAMED
Model / Reference
SUPERTA-E-90 EUDAMED

Identifiers

Primary DI / UDI-DI
85942023202782 EUDAMED
Basic UDI-DI
859420232LP01EP EUDAMED
Direct Marketing DI
85942023202782 EUDAMED
EMDN Code
V08060101 HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Basic electric hospital bed

Superta E by PROMA REHA, s.r.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic electric hospital bed.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
PROMA REHA, s.r.o.
EUDAMED SRN
CZ-MF-000013860

Sources (1)

  • EUDAMED cf8773fc-4371-4b63-8348-37d0b6f8b5e2 61 fields · synced Aug 5, 2026